Laurent Villard - Concepedia

Author

Laurent Villard

Also Known As

Célia Verley, G Plessis, Jean-Michel Pédespan, L Villard, L. Villard, LAURENT VILLARD, Laurent Villard, Nadine Jalkh, Silvana van Koningsbruggen, VILLARD, L

314

Publications

8.3K

Citations

H-Index

125

Concepts

All Affiliations

Inserm Aix-Marseille Université Hôpital de la Timone Centre National de la Recherche Scientifique Assistance Publique – Hôpitaux de Paris

About

Laurent Villard is an author at Inserm specializing in medicine, genetics, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	32	53	3.9K
2	Natural Sciences	4	4	131
3	Health Sciences	2	2	52
4	Public Health	2	2	78
5	Engineering	1	1	17

Laurent Villard

110

Publications

7.1K

Citations

H-Index

Page 1

	Year	Citations
Mutations in a putative global transcriptional regulator cause X-linked mental retardation with α-thalassemia (ATR-X syndrome) Richard J. Gibbons, David J. Picketts, Laurent Villard, Cell Transcriptional RegulationDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	1995	628
Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders Markus Wolff, Katrine M. Johannesen, Ulrike B. S. Hedrich, Brain	2017	558
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes Sabine Endele, Georg Rosenberger, Kirsten Geider, Nature Genetics Developmental BiologyMolecular NeuroscienceBrain DevelopmentNeuroanatomyGenetics	2010	502
Mecp2 Deficiency Disrupts Norepinephrine and Respiratory Systems in Mice Jean‐Charles Viemari, Jean‐Christophe Roux, Andrew K. Tryba, Journal of Neuroscience Mecp2-/y MiceNeurodegenerative DiseasesMolecular PhysiologyMendelian DisorderLung Inflammation	2005	281
Two affected boys in a Rett syndrome family Laurent Villard, Arlette Kpebe, Carlos Cardoso, Neurology	2000	194
Treatment with desipramine improves breathing and survival in a mouse model for Rett syndrome Jean‐Christophe Roux, Emmanuelle Dura, Anne Moncla, European Journal of Neuroscience	2007	140
Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype Pierre Cacciagli, Marie-Reine Haddad, Cécile Mignon‐Ravix, European Journal of Human Genetics Severe Neurological PhenotypeGenetic DisorderGeneticsMolecular GeneticsMolecular Neurobiology	2010	140
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complex Nadia Bahi‐Buisson, Karine Poirier, Nathalie Boddaert, Brain Neurodegenerative DiseasesMendelian DisorderGenetic DisorderCorticobasal DegenerationPathology	2010	140
Mutations in SLC13A5 Cause Autosomal-Recessive Epileptic Encephalopathy with Seizure Onset in the First Days of Life Julien Thévenon, Mathieu Milh, François Feillet, The American Journal of Human Genetics First DaysNeurobiology Of DiseaseNeurological DisorderGenetic DisorderGenetics	2014	133
Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion Carlos Cardoso, Amber Boys, Elena Parrini, Neurology	2008	129

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